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In research of other receptor tyrosine kinases implicated during the oncogenesis of GIST, nilotinib obtained powerful and selective inhibition of PDGFRα and PDGFRβ. As is the situation with imatinib, nilotinib potently inhibited the autophosphorylation of A31 cells reworked by PDGFRABased on nonlinear pharmacokinetic profile of nilotinib, growing